Chemistry Letters p. 1595 - 1598 (1982)
Update date:2022-07-30
Topics:
Suga, Takayuki
Hirata, Toshifumi
Lee, Ym Sook
In the biotransformation of the enantiomers of p-ment-1-en-8-ol (α-terpineol) and 8-acetoxy-p-ment-1-ene (α-terpinyl acetate) with the cultured suspension cells of Nicotina tabacum, it was clarified that the cultured cells effected the hydroxylation at the 6-position of (4R)-(+)-enantiomer in preference to the (4S)-(-)-enantiomer, whereas the cells did the hydrolysis of the acetoxyl group and the hydroxylation of the ethylenic linkage of (4S)-(-)-α-terpinyl acetate in preference to the (4R)-(+)-enantiomer.
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Doi:10.1007/BF00513427
(1982)Doi:10.1021/ja0433370
(2005)Doi:10.1016/S0022-328X(00)87086-2
(1982)Doi:10.1007/BF00506672
(1985)Doi:10.1039/jr9480000559
(1948)Doi:10.1021/ic048721c
(2005)
